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Results of search for 'au:"Fryns, J.-P."', page 13 of 56
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Authors
Borghgraef, M
Cassiman, J J
De Smet, L
Devriendt, K
Fryns, J P
Fryns, J-P
Kleczkowska, A
Legius, E
Lukusa, T
Moerman, P
Petit, P
Schrander-Stumpel, C
Swillen, A
Van Den Berghe, H
Van den Berghe, H
Vandenberghe, K
Vermeesch, J R
Vogels, A
Witters, I
van den Berghe, H
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Abnormalities, Multiple
Adolescent
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Child, Preschool
Chromosome Aberrations
Chromosome Deletion
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Humans
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Infant, Newborn
Intellectual Disability
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241.
Unilateral limb reduction defect and lumbar appendage: disorganisation-like syndrome?
[electronic resource]
by
Devriendt, K
Vandenbossche, L
Fryns, J P
Producer:
20040720
In:
Genetic counseling (Geneva, Switzerland)
vol. 15
Availability:
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242.
[Slight mental handicap and procreation. Knowledge and practice in 15 slightly mentally handicapped women].
[electronic resource]
by
Neve-Dumont, N
Busschaert, M
Fryns, J P
Producer:
19870212
In:
Soins. Psychiatrie
no. 72
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243.
Deletion of the short arm of the X chromosome: a hereditary form of Turner syndrome.
[electronic resource]
by
Massa, G
Vanderschueren-Lodeweyckx, M
Fryns, J P
Producer:
19930204
In:
European journal of pediatrics
vol. 151
Online resources:
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244.
A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?
[electronic resource]
by
Maximilian, C
Ioan, D M
Fryns, J P
Producer:
19920910
In:
Genetic counseling (Geneva, Switzerland)
vol. 3
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245.
Axial mesodermal dysplasia spectrum: variable symptoms in affected sibs.
[electronic resource]
by
Fryns, J P
Remans, P J
Fabry, G
Producer:
19930930
In:
American journal of medical genetics
vol. 46
Online resources:
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246.
Bilateral aplasia of the mandibular ramus and condyle in Klinefelter syndrome.
[electronic resource]
by
Fryns, J P
Carels, C
Schoenaers, J H
Producer:
19960731
In:
Genetic counseling (Geneva, Switzerland)
vol. 7
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247.
Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosis.
[electronic resource]
by
De Smet, L
Keymolen, K
Fryns, J P
Producer:
20000127
In:
Genetic counseling (Geneva, Switzerland)
vol. 10
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248.
Holoprosencephaly in deletions of proximal chromosome 14q.
[electronic resource]
by
Devriendt, K
Fryns, J P
Chen, C P
Producer:
19981001
In:
Journal of medical genetics
vol. 35
Online resources:
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249.
Bilateral aplasia of the thumb, proximal radioulnar synostosis and unilateral synostosis of metacarpals 4 and 5.
[electronic resource]
by
Debeer, Ph
De Smet, L
Fryns, J P
Producer:
20040720
In:
Genetic counseling (Geneva, Switzerland)
vol. 15
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250.
Syndromes presenting adducted thumb with/without clubfoot and Dundar syndrome.
[electronic resource]
by
Uzak, A Subasioglu
Fryns, J P
Dundar, M
Producer:
20140812
In:
Genetic counseling (Geneva, Switzerland)
vol. 25
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251.
Madelung deformity as a pathognomonic feature of the onycho-osteodysplasia syndrome.
[electronic resource]
by
Ioan, D M
Maximilian, C
Fryns, J P
Producer:
19920701
In:
Genetic counseling (Geneva, Switzerland)
vol. 3
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252.
Mandibuloacral dysplasia as a form of idiopathic osteolysis.
[electronic resource]
by
Fryns, J P
Schrander-Stumpel, C
Spaepen, A
Producer:
19920624
In:
Pediatric radiology
vol. 21
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253.
A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
[electronic resource]
by
van Buggenhout, G
Decock, P
Fryns, J P
Producer:
19960731
In:
Genetic counseling (Geneva, Switzerland)
vol. 7
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254.
Three young children with Smith-Magenis syndrome: their distinct, recognisable behavioural phenotype as the most important clinical symptoms.
[electronic resource]
by
Willekens, D
De Cock, P
Fryns, J P
Producer:
20001121
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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255.
Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal father.
[electronic resource]
by
De Smet, L
Devriendt, K
Fryns, J P
Producer:
20020213
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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256.
Intrafamilial clinical variability in type C brachydactyly.
[electronic resource]
by
Debeer, P
De Smet, L
Fryns, J P
Producer:
20020723
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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257.
Choroid plexus cysts and oligohydramnios: presenting echographic signs in a female fetus with deletion of the Wolf-Hirschhorn syndrome region (4p16.3).
[electronic resource]
by
Witters, I
Van Schoubroeck, D
Fryns, J P
Producer:
20020723
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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258.
Nuchal edema as the first sign of fetal valproate syndrome.
[electronic resource]
by
Witters, I
Van Assche, F
Fryns, J P
Producer:
20030211
In:
Prenatal diagnosis
vol. 22
Online resources:
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259.
Dysmorphology in literature: describing is not condoning.
[electronic resource]
by
Adib, S M
Mégarbané, A
Fryns, J P
Producer:
20030827
In:
Genetic counseling (Geneva, Switzerland)
vol. 14
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260.
Cytomegalovirus reactivation in pregnancy and subsequent isolated bilateral hearing loss in the infant.
[electronic resource]
by
Witters, I
Van Ranst, M
Fryns, J P
Producer:
20010215
In:
Genetic counseling (Geneva, Switzerland)
vol. 11
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